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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791828Generated: October 26, 2026

Nitric Acid → Ethyl 5-hydroxy-4-nitroindole-2-carboxylate

https://huagongshe.com/reaction/1791828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantEthyl 5-methoxyindole-2-carboxylateHCID 20926—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-hydroxy-4-nitroindole-2-carboxylateHCID 2203061259%

Reaction Steps

A mixture of ethyl 5-methoxyindole-2-carboxylate (8.15 g, 37.2 mmol), (prepared by the method described in Heterocycles Vol. 43, No. 2, p. 263–266), nitric acid adsorbed on silica gel (24 g) and dichloromethane (150 ml) was stirred at ambient temperature for 18 hours. The dichloromethane was removed in vacuo and the product washed off the silica with acetone. The acetone was evaporated in vacuo. The residue was treated again with nitric acid on silica (1 g) as above and the work up procedure repeated to give ethyl 5-hydroxy-4-nitroindole-2-carboxylate (5.8 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-c0d5244af2d04652bf6b3bc60250d25d
Source noteuspto-grants-2006_07